Transmissible Viral Vaccines... how the shots are affecting those who haven't taken it. They may be designed to do exactly that

Nemo

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Dr. Baker discusses environmental transmission. I believe he is a chiropractor. He is no longer accepting patients who've gotten the vax.

He's maybe a tad excitable, but talks about how, when you breathe, you exhale your own cells, and points out viruses are smaller than cells. We've seen microscopic photographs of covid virus particles, and obviously the spike proteins are smaller still.


View: https://www.bitchute.com/video/3OfBPUZ2U0Wy/


Here's a study of the cr*p you exhale with every breath. Lots and lots of particles of all kinds, proteins, lipids, all kinds of junk.

 

Rick K

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Probably heroin doesn't migrate to all of your skin cells the way the vax mRNA does.
Besides, if a drug could jump this way we'd all be on ssri's and antibiotics. Shedding is the way viruses jump hosts. Drugs aren't alive and don't need to go anywhere.
 

Nemo

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New discussion of Bat Plague vax studies has a lot of new material.

It has a more in-depth discussion of the vax' contents than I've seen before, plus in-depth discussion of the nanolipids and PEG coating, the ADE issue, and the Mad Cow prions.

They discuss emergence of new Covid strains as a result of the vaxxes. Richard M. Fleming MD PhD JD was sounding the alarm about this back in January and he seems to have been proven right. Essentially immune-compromised people are breeding grounds for new strains resistant to the antibodies produced by the vaxxes. They predict there will be more calls for new rounds of shots every few months, and it will be "an arms race that we will probably lose."

They also discuss studies supporting environmental transmission, and a plausible process by which exosomes from dendritic cells in the spleen containing misfolded spike proteins may be transmitted via exhalation and other methods from vaxxed to unvaxxed people.


The discussion was written by Stephanie Seneff, who works at the Computer Science and Artificial Intelligence Laboratory at MIT, and Dr. Nigh, who specializes in Naturopathic Oncologogy at Immerson Health in Portland, Oregon. It was released this week in the International Journal of Vaccine Theory, Practice, and Research, and devotes a considerable space to discussing the research of Dr. J. Bart Classen, who first published a research paper on the possibility of prion-linked brain degeneration caused by the COVID-19 vaccine last month.

If you remember, Fleming discussed a study of his colleague, Kevin McCullough, with macaques, in which 100% of the monkeys got Mad Cow from the prion portion of the spike protein. Same with another study on humanized mice.

I think you'll be interested in this paper. 42 pages.
 
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Nemo

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New discussion of Bat Plague vax studies has a lot of new material.

First thing we learn was there was only a 2% likelihood of the mRNA vaxxes making it through Stage 2 (efficacy) and Stage 3 (population benefit) trials.

Yet we suddenly have these vaxxes with purported 90-95% efficacy. The British Medical Journal has been giving a platform to prominent voices challenging these efficacy claims and the authors of this review go through the ways the data appear to have been fudged.

Among other things, using the vax makers' own data (which again, appears to be rigged), the absolute risk reduction of the Moderna vaccine was only 1.1%. For the Pfizer vax, it was only 0.7%.
 

Nemo

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First thing we learn was there was only a 2% likelihood of the mRNA vaxxes making it through Stage 2 (efficacy) and Stage 3 (population benefit) trials.

Here's something troubling (p. 7). They slightly modified the spike protein to favor a stable configuration in its prefusion state. That's meant to provoke a stronger immune response.

But this might also mean the spike protein produced by the human host cell lingers in the plasma membrane bound to ACE2 receptors because of its impaired fusion capability. And we don't know what the effect of that would be.

Also, several experiments showed that producing spike protein alone failed to initiate a T cell response in animal studies. Yet the mRNA vaxxes contain only mRNA to produce the spike protein, despite its observed poor performance.
 

akgrrrl

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Here's something troubling (p. 7). They slightly modified the spike protein to favor a stable configuration in its prefusion state. That's meant to provoke a stronger immune response.

But this might also mean the spike protein produced by the human host cell lingers in the plasma membrane bound to ACE2 receptors because of its impaired fusion capability. And we don't know what the effect of that would be.

Also, several experiments showed that producing spike protein alone failed to initiate a T cell response in animal studies. Yet the mRNA vaxxes contain only mRNA to produce the spike protein, despite its observed poor performance.
I learned more from reading this well-written piece than anything else to date. Thank you for all you do for the RPF.
 

Nemo

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But this might also mean the spike protein produced by the human host cell lingers in the plasma membrane bound to ACE2 receptors because of its impaired fusion capability. And we don't know what the effect of that would be.

Regarding the polyethylene glycol (PEG) modified lipid nanoparticles, a study showed that small doses (such as the vaccine dose) can lead to dramatic pathological immune activation. In animal studies, it was responsible for anaphylaxis and cardiovascular collapse. In pigs, it occurred only after the second injected exposure. (p. 11).

Also, up to 72% of the population with no previous PEG-based medical therapy has anti-PEG antibodies. Not only does that lead to severe adverse effects but also to impaired therapeutic efficacy.

One study concluded, "PEG is a high risk 'hidden' allergen." There's a high risk of inadvertent re-exposure, which leads to more severe adverse reactions. They concluded it should only be used in specialist drug allergy centers.

While anaphylactic reactions to other vaccines averages 2 per million recipients, 2.1% have acute allergic reactions to mRNA vaxxes. A more extreme anaphylactic reaction occurred in 247 per million recipients. Second exposures will result in higher numbers.
 
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Nemo

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Regarding the polyethylene glycol (PEG) modified lipid nanoparticles, a study showed that small doses (such as the vaccine dose) can lead to dramatic pathological immune activation. In animal studies, it was responsible for anaphylaxis and cardiovascular collapse.

There's a great opening paragraph to the Antibody-Dependent Enhancement (ADE) section. ADE is essentially where you create antibodies that actually enhance cell infectivity. It was first described in a study in 1964. Because nobody could figure out how this could happen, ADE was forgotten for 20 years.

ADE would mean the antibodies produced by the vaxxes were insufficient to neutralize the virus upon reexposure. (When you look at the weak antibody response to vaxxes that produced only the spike protein, like the vaxxes people are actually getting, this is a real concern.) Nevertheless, they'd bind with the virus, facilitating viral entry into cells and producing even worse illness.

In the Nature Biotechnology journal, Eroshenko et al offered a comprehensive review of evidence that ADE could become manifest with any Bat Plague vax. It's already been observed in vitro and in vivo with other coronavirus vaccines.

So this is yet more support for the claims of microbiologist/immunologist Dolores Cahill and many other doctors and scientists, and it's not just from the Eroshenko group.
 

Nemo

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ADE would mean the antibodies produced by the vaxxes were insufficient to neutralize the virus upon reexposure. (When you look at the weak antibody response to vaxxes that produced only the spike protein, like the vaxxes people are actually getting, this is a real concern.) Nevertheless, they'd bind with the virus, facilitating viral entry into cells and producing even worse illness.

This section just gets worse from there. For example, a 2019 study showed preexisting immunoglobulin antibodies, induced by prior vaccination, contributed to severe pulmonary damage by Bat Plague in macaques.

And ay caramba, a 2020 study shows this effect is likely to be far worse in the elderly because of their long history of diverse exposures to previous coronaviruses!

And good grief! This effect might be triggered by the booster shots they are calling for in the already-vaxxed!
 

Nemo

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This section just gets worse from there. For example, a 2019 study showed preexisting immunoglobulin antibodies, induced by prior vaccination, contributed to severe pulmonary damage by Bat Plague in macaques.

The cherry on the ADE sundae:

Antibodies to the spike protein (the expected outcome of the Bat Plague shots) have been found to produce high levels of cross-reactive antibodies against endogenous human proteins!

This may manifest as either acute or chronic autoimmune and inflammatory conditions.

On p. 15, you can see tissues likely to be attacked (a Peater's nightmare): tTG (associated with celiac disease), TPO (Hashimoto's), myelin basic protein (multiple sclerosis). Also liver tissue, mitochondria, nervous system, digestive system, and the pancreas.

And that's not all. It goes on and on. They point out that Dr. Gregory Michael died of cerebral hemorrhage 16 days after his first Pfizer shot. Within 3 days of the vax, he had developed idiopathic thrombocytopenic purpura. That's an autoimmune disorder where his immune cells were attacking his own platelets.
 
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Lollipop2

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New discussion of Bat Plague vax studies has a lot of new material.

It has a more in-depth discussion of the vax' contents than I've seen before, plus in-depth discussion of the nanolipids and PEG coating, the ADE issue, and the Mad Cow prions.

They discuss emergence of new Covid strains as a result of the vaxxes. Richard M. Fleming MD PhD JD was sounding the alarm about this back in January and he seems to have been proven right. Essentially immune-compromised people are breeding grounds for new strains resistant to the antibodies produced by the vaxxes. They predict there will be more calls for new rounds of shots every few months, and it will be "an arms race that we will probably lose."

They also discuss studies supporting environmental transmission, and a plausible process by which exosomes from dendritic cells in the spleen containing misfolded spike proteins may be transmitted via exhalation and other methods from vaxxed to unvaxxed people.


The discussion was written by Stephanie Seneff, who works at the Computer Science and Artificial Intelligence Laboratory at MIT, and Dr. Nigh, who specializes in Naturopathic Oncologogy at Immerson Health in Portland, Oregon. It was released this week in the International Journal of Vaccine Theory, Practice, and Research, and devotes a considerable space to discussing the research of Dr. J. Bart Classen, who first published a research paper on the possibility of prion-linked brain degeneration caused by the COVID-19 vaccine last month.

If you remember, Fleming discussed a study of his colleague, Kevin McCullough, with macaques, in which 100% of the monkeys got Mad Cow from the prion portion of the spike protein. Same with another study on humanized mice.

I think you'll be interested in this paper. 42 pages.
Solid find here @Nemo! Thank you. Already sent it off to some vaxxed people I know.

The problem is those who have been vaxxed don’t want to hear about this or read negative truths about the injections. They staunchly defend their right to have been vaxxed, just like the lady with cancer in the other thread. You nailed it in your response-brutal for a woman like that but true. Your voice carries weight as someone who overcame cancer as well. She totally ignored my post about having problems 12 or 18 months later when exposed to other Coronaviruses or from the flu vaccine.

If just one person rethinks getting the injection, they all our efforts will be worth it.
 

Rick K

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The cherry on the ADE sundae:

Antibodies to the spike protein (the expected outcome of the Bat Plague shots) have been found to produce high levels of cross-reactive antibodies against endogenous human proteins!

This may manifest as either acute or chronic autoimmune and inflammatory conditions.
I believe this to be a part of the "Plan". We will become wholly dependent on big pharma for new cures to sustain life once we have chronic autoimmune conditions.
 

Lollipop2

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I believe this to be a part of the "Plan". We will become wholly dependent on big pharma for new cures to sustain life once we have chronic autoimmune conditions.
This rings true to me. Honestly this has worked brilliantly for all of the other vaccines, why wouldn’t it with these injections? The amount of allergies, chronic disease, brain and neurological illnesses, cancers and on and on can be traced back to the horrific CDC vaccine schedule in the US.
 

Nemo

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On p. 15, you can see tissues likely to be attacked (a Peater's nightmare): tTG (associated with celiac disease), TPO (Hashimoto's), myelin basic protein (multiple sclerosis). Also liver tissue, mitochondria, nervous system, digestive system, and the pancreas.

On p. 17, you can see where the mRNA travels from the injection site. It goes everywhere. First to your lymph nodes, then heavily to your spleen and liver, but also to your blood, lungs, brain, etc.

Depending on the vax you got, your nanoparticles may accumulate in one organ, and other vax material in other organs.
 

Nemo

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I believe this to be a part of the "Plan". We will become wholly dependent on big pharma for new cures to sustain life once we have chronic autoimmune conditions.

Rick, right. If you've gotten one vax, and it's known to be relatively weak and mostly worn off in 8ish weeks, you almost have to get a second vax to have enough antibodies to kill the virus, because otherwise ADE.

But if you get the second vax, and then the third, 4th, and so on, you're at risk of triggering your own ADE.

And if you had a strong immune system, so that you never noticed you got Covid, you could trigger ADE by getting the vax.
 

Nemo

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On p. 17, you can see where the mRNA travels from the injection site. It goes everywhere. First to your lymph nodes, then heavily to your spleen and liver, but also to your blood, lungs, brain, etc.

They think the autoimmune thrombocytopenia (ITP), an important complication of Covid and also of the shots, may result from a migration of immune cells carrying a cargo of mRNA nanoparticles via the lymph system into the spleen. The immune cells would produce spike protein there and the spike protein would induce B cell generation IgG antibodies to it.

There can then be a signalling cascade that suppressed megakaryocyte production in the bone marrow. In other words, the problem is suppression of platelet production, not platelet destruction.

Again, it's ITP that's producing all those crashes in platelet counts we're seeing.

They then go into a long section on suppressed autophagy. Summary: Not good!
 
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